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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Structural characterization of a pectic polysaccharide from Codonopsis pilosula and its immunomodulatory activities in vivo and in vitro
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Structural characterization of a pectic polysaccharide from Codonopsis pilosula and its immunomodulatory activities in vivo and in vitro

机译:Codonopsis pilosula的果糖性多糖及其体内免疫调节活动的结构表征

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摘要

A pectic polysaccharide (named as CPP1c) extracted from Codonopsis pilosula was evaluated for its structural features and potential of immune-modulating activities in an aging mouse model of senescence accelerated mouse prone 8 (SAMP8) in vitro and in vivo. The relative molecular weight and the absolute molecular weight of CPPlc were 1.26 x 10(5) Da and 1.49 x 10(5) Da, respectively. Investigation of structural features by a combination of chemical and instrumental analysis showed CPPIc was composed of -> 1)-alpha-L-Rhap-(2,4 ->,-> 1)-alpha-L-Araf-(5 ->,-> 1)-alpha-D-Galp-(6 -> and -> 1)-alpha-D-GalpA-(4 -> in a molar ratio of 3:1:2:33. CPP1 c could promote lymphocyte proliferation, modulate the percentage of CD4(+), CDS8(+), CD28(+) and CD152(+) T cells and enhance the production of IL-2, TNF-alpha and IFN-gamma. Moreover, PCR assay revealed CPPlc augmented the expressions of CD28, PI3 K and p38MAPK mRNA, and the increase of protein expressions of the same genes was also confirmed by western blot analyses. In addition, CPPlc had the potential of promoting the homing of lymphocytes. Taking all factors into consideration, we deduced CPPl c might exert its immunostimulating potency via promoting T cell activation by TCR/CD28 signaling pathways. (C) 2017 Published by Elsevier B.V.
机译:评价从Codonopsis pilosula中提取的果糖(命名为CPP1C),用于其在体外和体内衰老的小鼠易一(SAMP8)的老化小鼠模型中的结构特征和免疫调节活动的潜力。 CPPLC的相对分子量和绝对分子量分别为1.26×10(5)达,分别为1.49×10(5)达达。通过化学和仪器分析的组合对结构特征进行了研究表明,CPPIC由 - > 1) - α-L-RHAP-(2,4 - >, - > 1) - alpha-L-ARAF-(5 - > , - > 1) - alpha-d-galp-(6 - >和 - > 1)-alpha-d-galpa-(4 - >以摩尔比为3:1:2:33。CPP1 C可以促进淋巴细胞增殖,调节CD4(+),CdS8(+),CD28(+)和CD152(+)T细胞的百分比,增强IL-2,TNF-α和IFN-γ的产生。此外,PCR测定显示CPPLC增强CD28,PI3 K和P38MAPK mRNA的表达,并通过Western印迹分析证实了相同基因的蛋白质表达的增加。此外,CPPLC有可能促进淋巴细胞归巢。考虑所有因素,我们推导过CPPL C可能通过TCR / CD28信号传导途径促进T细胞激活来发挥其免疫刺激效力。(c)2017由elestvier bv发布

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